HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728856Generated: October 30, 2026
Triethyl phosphite → HCID 21667292, compound
https://huagongshe.com/reaction/728856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | HCID 21667325 | HCID 21667325 | — |
| Reactant | HCID 53907037 | HCID 53907037 | — |
| Product | HCID 21667292 | HCID 21667292 | — |
Reaction Steps
The starting material is manufactured as follows: 5-Methyl-5-vinyl-2-oxazoline-4-carboxylic acid ethyl ester, b.p. 65°-75° (13 Pa) is obtained by reaction of isocyanoacetic acid ethyl ester with methyl vinyl ketone in a manner analogous to that described in Example 30. By hydrolysis of the 5-methyl-5-vinyl-2-oxazoline-4-carboxylic acid ethyl ester in a manner analogous to that described in Example 1, 2-formylamino-3-hydroxy-3-methyl-4-pentenoic acid ethyl ester is obtained.Reaction of the 2-formylamino-3-hydroxy-3-methyl-4-pentenoic acid ethyl ester with thionyl bromide and subsequent treatment with triethyl phosphite in a manner analogous to that described in Example 1 yields E-2-formylamino-3-methyl-5-diethylphosphono-3-pentenoic acid ethyl ester in the form of a colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051413 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-c245f89843804025a501f487a4be5120 |
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| Source note | uspto-grants-1991_09 |
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